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Unusual accumulation of sulfated glycosphingolipids in colon cancer cells

机译:硫酸化糖鞘脂在结肠癌细胞中的异常积累

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The structures of glycosphingolipids from highly purified colorectal cancer cells and normal colorectal epithelial cells of 16 patients have been analyzed in fine detail (Misonou Y, Shida K, Korekane H, Seki Y, Noura S, Ohue M, Miyamoto Y. 2009. Comprehensive Clinico-Glycomic Study of 16 Colorectal Cancer Specimens: Elucidation of aberrant glycosylation and ts mechanistic causes in colorectal cancer cells. J Proteome Res. 8:2990–3005). Further structural analyses demonstrated that colon cancer cells from two patients accumulated unusual glycosphingolipids which were not observed in either colorectal cancer cells or normal colorectal epithelial cells from the other patients. Mass spectrometry analyses revealed that the unusual structures include sulfated oligosaccharides. The structures of the glycosphingolipids of the cancer cells from these two cases were analyzed by methods which include enzymatic release of carbohydrate moieties, fluorescent labeling with aminopyridine and identification using two-dimensional mapping, enzymatic digestion and mass spectrometry together with methanolysis, and the use of newly synthesized sulfo-fucosylated oligosaccharides as standards. The colon cancer cells from one of the patients demonstrate a variety of oligosaccharides as major components which are sulfated at the C6 position of subterminal GlcNAc and at C3 positions of terminal galactose with or without sialylation or fucosylation. These include 6-sulfo Lex, 6′-sialyl 6-sulfo lactosamine, and 3′-sialyl 6-sulfo Lex, in addition to sialylated or fucosylated derivatives of type-1 and type-2 hybrid oligosaccharides. The colon cancer cells from the other patient have two kinds of sulfated oligosaccharides, a 6-sulfo Lex structure and a 3′-sulfo Lex structure, as minor components. Taking into consideration the clinical features of the two patients, the biological significance of sulfated glycosphingolipids on cancer cells is discussed.
机译:已对16例患者的高纯度结直肠癌细胞和正常结直肠上皮细胞糖鞘脂的结构进行了详细分析(Misonou Y,Shida K,Korekane H,Seki Y,Noura S,Ohue M,Miyamoto Y.2009。综合临床-对16个大肠癌标本的糖酵解研究:阐明大肠癌细胞中异常糖基化和ts机理的原因(J Proteome Res。8:2990–3005)。进一步的结构分析表明,两名患者的结肠癌细胞积聚了异常的鞘糖脂,这在其他患者的结直肠癌细胞或正常结直肠上皮细胞中均未观察到。质谱分析显示异常结构包括硫酸化的低聚糖。通过以下方法分析了这两种情况下癌细胞的鞘糖脂的结构,这些方法包括酶促释放碳水化合物部分,用氨基吡啶进行荧光标记和使用二维作图进行鉴定,酶消化和质谱分析以及甲醇分解,以及使用新合成的磺基岩藻糖基化寡糖为标准品。来自一名患者的结肠癌细胞表现出多种低聚糖作为主要成分,它们在有或没有唾液酸化或岩藻糖基化的情况下在亚末端GlcNAc的C6位和半乳糖末端的C3位被硫酸化。除唾液酸化或岩藻糖基化衍生物外,还包括6-磺基Le x ,6'-唾液酸基6-磺基乳糖胺和3'-唾液酸基6-硫基Le x 。 1型和2型杂合寡糖。另一例患者的结肠癌细胞具有两种硫酸化的低聚糖,即6-巯基Le x 结构和3'-磺基Le x 结构作为次要成分。考虑到两名患者的临床特征,讨论了硫酸糖鞘脂在癌细胞上的生物学意义。

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    《Glycobiology》 |2009年第9期|p.1018-1033|共16页
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    2Department of Immunology, Osaka Medical Center for Cancer and Cardiovascular Diseases, 1-3-2 Nakamichi, Higashinari-ku, Osaka 537-8511 3Department of Disease Glycomics, The Institute of Scientific and Industrial Research, Osaka University, 8-1 Mihogaoka, Ibaraki, Osaka 567-0047 4Department of Surgery, Osaka Medical Center for Cancer and Cardiovascular Diseases, 1-3-3 Nakamichi, Higashinari-ku, Osaka 537-8511 5Department of Biochemistry 6Kochi System Glycobiology Center, Kochi University Medical School, Nankoku, Kochi 783-8505 7CREST, Japan Science and Technology Agency, Kawaguchi, Japan;

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